WT1 gene homepage

General information
Gene symbol WT1
Gene name WT1 transcription factor
Chromosome 11
Chromosomal band p13
Imprinted Unknown
Genomic reference LRG_525
Transcript reference NM_000378.4, NM_001198551.1, NM_001198552.1, NM_024424.3, NM_024426.4
Associated with diseases DDS, FRSR, MCHM, NPHS4, WT1
Citation reference(s) -
Curators (1) Despoina Kalfakakou
Total number of public variants reported 114
Unique public DNA variants reported 39
Individuals with public variants 135
Hidden variants 0
Date created May 20, 2020
Date last updated June 05, 2020
Version WT1:200605

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 12796
Entrez Gene 7490
PubMed articles WT1
OMIM - Gene 607102
OMIM - Diseases DDS (Denys-Drash syndrome)
FRSR (Frasier syndrome)
MCHM (Meacham syndrome)
NPHS4 (Nephrotic syndrome, type 4)
WT1 (Wilms Tumor 1)


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000237 11 Wilms tumor 1, transcript variant A NM_000378.4 NP_000369.3 114
00000238 11 Wilms tumor 1, transcript variant B NM_024424.3 NP_077742.2 114
00000239 11 Wilms tumor 1, transcript variant D NM_024426.4 NP_077744.3 114
00000240 11 Wilms tumor 1, transcript variant E NM_001198551.1 NP_001185480.1 114
00000241 11 Wilms tumor 1, transcript variant F NM_001198552.1 NP_001185481.1 114


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